IP Library Granted Patent US 8,993,731
Granted Patent B2
US 8,993,731 · App. 13/583,999 · Granted Mar 31, 2015

PD-1 antibody

Inventor: Kerry Louise Tyson (Reading, GB)
Assignee: UCB Biopharma SPRL
C07K16/2803C07K16/2818A61K39/3955A61K45/06C07K2317/24C07K2317/567C07K2317/75C07K2317/92C07K2319/30
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 8,993,731
App. No.
13/583,999
Granted
Mar 31, 2015
Kind
B2
Abstract

A humanized agonistic antibody which binds human PD-1 comprising a heavy chain wherein the variable domain of the heavy chain comprises the sequence given in SEQ ID NO:1 for CDR-H1, the sequence given in SEQ ID NO: 2 for CDR-H2 and the sequence given in SEQ ID NO: 3 for CDR-H3 and the heavy chain framework region is derived from human sub-group sequence VH4 3-1 4-30.4+JH4 (SEQ ID NO: 33). The disclosure also extends to therapeutic uses of the antibody molecules, compositions and methods for producing said antibody molecules.

Claims (17)

1. A humanised agonistic antibody which binds human PD-1 comprising a heavy chain wherein the variable domain of the heavy chain comprises the sequence given in SEQ ID NO:1 for CDR-H1, the sequence given in SEQ ID NO:2 for CDR-H2 and the sequence given in SEQ ID NO:3 for CDR-H3 and the heavy chain framework region is human sub-group sequence VH4 3-1 4-30.4+JH4 (SEQ ID NO: 33) or a derivative thereof wherein up to four residues are changed.

2. A humanised antibody according to claim 1 wherein the residue at at least one of positions 25, 44, 48 and 71 of the variable domain of the heavy chain, as numbered according to Kabat, is a donor residue.

3. A humanised antibody according to claim 2 having the heavy chain variable domain sequence given in SEQ ID NO:23.

4. The antibody of claim 1 further comprising a light chain wherein the variable domain of the light chain comprises the sequence given in SEQ ID NO:4 for CDR-L1, the sequence given in SEQ ID NO:5 for CDR-L2 and the sequence given in SEQ ID NO:6 for CDR-L3 and the light chain framework region is human sub-group sequence VK2 4-1-1 A18+JK2 (SEQ ID NO:31) or a derivative thereof wherein up to five residues are changed.

5. A humanised antibody according to claim 4 wherein the residue at at least one of positions 2, 3, 45, 62, and 87 of the variable domain of the light chain, as numbered according to Kabat, is a donor residue.

6. A humanised antibody according to claim 5 having the light chain variable domain sequence given in SEQ ID NO:15.

7. The antibody of claim 1 having a heavy chain comprising a sequence given in SEQ ID NO:23 and a light chain comprising a sequence given in SEQ ID NO:15.

8. An agonistic antibody molecule according to any one of claims 1 , 4 , or 7 , wherein the antibody molecule is selected from the group consisting of: a complete antibody molecule having full length heavy and light chains, an Fab, Fab′, F(ab′) 2 , Fv, VH, VL and scFv fragment.

9. A humanised agonistic antibody which binds human PD-1, wherein the variable domain of the light chain comprises a sequence having at least 95% identity to a light chain variable domain comprising a sequence given in SEQ ID NO:15 and wherein the variable domain of the heavy chain comprises a sequence having at least 95% identity to a heavy chain variable domain comprising a sequence given in SEQ ID NO:23.

10. An isolated DNA sequence encoding the heavy and/or light chain(s) of an antibody according to any one of claims 1 , 4 , or 7 .

11. A cloning or expression vector comprising one or more DNA sequences according to claim 10 .

12. A cultured host cell comprising one or more cloning or expression vectors according to claim 11 .

13. A process for the production of the antibody comprising culturing the host cell of claim 12 and isolating the antibody.

14. The antibody according to claim 8 , wherein the antibody is conjugated to one or more effector molecules.

15. A pharmaceutical composition comprising an antibody according to any one of claims 1 , 4 , 7 , or 14 in combination with one or more of a pharmaceutically acceptable excipient, diluent or carrier.

16. A pharmaceutical composition according to claim 15 , additionally comprising other active ingredients.

17. The pharmaceutical composition according to claim 16 , wherein the active ingredients are selected from the group consisting of: an antibody, anti-TNF, anti-IL-1β, anti-T cell, anti-IFNγ, anti-LPS, a xanthine, a corticosteroid, fluticasone propionate, a beta-2-agonist, salbutamol, salmeterol, formoterol, an inhibitor of cell growth and proliferation, rapamycin, cyclophosphamide, methotrexate, a CD28 inhibitor and a CD40 inhibitor.

Assignments (2)
CORRECTIVE ASSIGNMENT TO CORRECT THE DESIGNATION ON COVER SHEET PREVIOUSLY RECORDED AT REEL: 034738 FRAME: 0645. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Mar 9, 2015
From: TYSON, KERRY LOUISE
To: UCB BIOPHARMA SPRL
Reel/Frame 035176/0646 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 16, 2015
From: TYSON, KERRY LOUISE
To: UCB BIOPHARMA SPRL
Reel/Frame 034738/0645 →
Continuity (2)
Provisional Application 61312754 · Mar 11, 2010
Related Publication 20130095098A1 · Apr 18, 2013